<HashMap><database>biostudies-arrayexpress</database><scores/><additional><submitter>Nicolas Germain</submitter><organism>Homo sapiens</organism><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/E-MTAB-15359</full_dataset_link><description>Recapitulate the myeloid sarcoma gene expression using Gelma hydrogels in leukemic cell lines RNA-seq was performed onleukemic cell lines K562, Molm-13, PL-21, OCI-AML under two conditions (GelMA and control) to assess differential gene expression related to phenotype.</description><repository>biostudies-arrayexpress</repository><sample_protocol>Sample Collection - Cell lines were analyzed after 15 days of culture in suspension. Cells within GelMA 5% hydrogels were collected after dissociation with collagenase type I. All samples were stored at −80 °C until RNA extraction.</sample_protocol><sample_protocol>Library Construction - RNA libraries were prepared using the AccuraCode RNA-Seq Kit (Cat. no. 10710174, Singleron Biotechnologies GmbH) following the manufacturer’s instructions. Polyadenylated mRNA was isolated using AccuraCode beads (Cat. no. 1200030080). cDNA was synthesized with sample-specific barcodes and unique molecular identifiers (UMIs), pooled, and amplified to construct sequencing libraries.</sample_protocol><sample_protocol>Sequencing - Sequencing was performed on an Illumina NovaSeq X platform using paired-end 150 bp reads, following the manufacturer’s protocol.</sample_protocol><sample_protocol>Nucleic Acid Extraction - Total RNA was extracted using the Quick-RNA Microprep Kit (Zymo Research, Irvine, CA, USA) according to the manufacturer’s protocol. RNA quantity and purity were assessed with a NanoDrop spectrophotometer (260/280 and 260/230 ratios), and RNA integrity was evaluated using an Agilent 2100 Bioanalyzer with an RNA 6000 Nano Kit. Only samples with RNA Integrity Number (RIN) greater than 7 were retained for library preparation</sample_protocol><figure_sub>Organization</figure_sub><figure_sub>MINSEQE Score</figure_sub><figure_sub>Assays and Data</figure_sub><figure_sub>Processed Data</figure_sub><figure_sub>MAGE-TAB Files</figure_sub><data_protocol>Data Transformation - Raw reads were demultiplexed, trimmed, and aligned to the human GRCh38 reference genome using STAR. Read counts were generated using featureCounts and normalized using the DESeq2 median-of-ratios method.</data_protocol><omics_type>Unknown</omics_type><omics_type>Transcriptomics</omics_type><omics_type>Genomics</omics_type><omics_type>Proteomics</omics_type><instrument_platform>Microprep kit</instrument_platform><instrument_platform>Illumina NovaSeq X</instrument_platform><instrument_platform>accuracode RNA-seq Kit</instrument_platform><study_type>RNA-seq of coding RNA</study_type><species>Homo sapiens</species><pubmed_authors>Nicolas Germain</pubmed_authors></additional><is_claimable>false</is_claimable><name>Transcriptome profiling of myeloid cell lines in Gelatin Methacrylate Hydrogels</name><description>Recapitulate the myeloid sarcoma gene expression using Gelma hydrogels in leukemic cell lines RNA-seq was performed onleukemic cell lines K562, Molm-13, PL-21, OCI-AML under two conditions (GelMA and control) to assess differential gene expression related to phenotype.</description><dates><release>2025-09-01T00:00:00Z</release><modification>2025-09-01T01:02:27.514Z</modification><creation>2025-07-14T13:37:21.264Z</creation></dates><accession>E-MTAB-15359</accession><cross_references><ENA>ERP176757</ENA><EFO>EFO_0002944</EFO><EFO>EFO_0004170</EFO><EFO>EFO_0005518</EFO><EFO>EFO_0003816</EFO><EFO>EFO_0003738</EFO><EFO>EFO_0004184</EFO></cross_references></HashMap>